Background: Recently, shock teams have been introduced to optimize cardiogenic shock (CS) care; however, their clinical benefits remain unclear. We conducted a systematic review and meta-analysis to assess whether management by a shock team improves outcomes in patients with CS.
Methods and results: This meta-analysis was conducted according to the PRISMA guidelines. Studies comparing adults with CS managed with or without a shock team were identified from the PubMed, Web of Science, and Cochrane Library databases. The primary outcome was short-term mortality (cardiac intensive care unit, in-hospital, or 30-day mortality); the secondary outcome was bleeding. Of the 7 retrospective cohort studies that met the inclusion criteria, 3 without a critical risk of bias were included in the analysis. Shock team management was significantly associated with lower short-term mortality (odds ratio [OR] 0.52; 95% confidence interval [CI] 0.32-0.85; P=0.010) and bleeding complications (OR 0.62; 95% CI 0.43-0.91; P=0.010). Sensitivity analysis using crude data also supported the mortality benefit (OR 0.68; 95% CI 0.54-0.85; P<0.010). However, no randomized trials were included, and the certainty of evidence was rated very low owing to the risk of bias and inconsistency.
Conclusions: Shock team management may improve short-term outcomes in patients with CS; however, the level of evidence is very low. Further prospective studies are needed to evaluate optimal shock team composition and roles.
背景:最近,休克小组被引入来优化心源性休克(CS)的护理;然而,它们的临床益处尚不清楚。我们进行了一项系统回顾和荟萃分析,以评估休克小组的治疗是否能改善CS患者的预后。方法和结果:本荟萃分析按照PRISMA指南进行。从PubMed、Web of Science和Cochrane Library数据库中确定了比较有或没有休克治疗的成人CS的研究。主要终点是短期死亡率(心脏重症监护病房、住院或30天死亡率);次要结果是出血。在符合纳入标准的7项回顾性队列研究中,3项没有严重偏倚风险的研究被纳入分析。休克组管理与较低的短期死亡率(优势比[OR] 0.52; 95%可信区间[CI] 0.32-0.85; P=0.010)和出血并发症(优势比[OR] 0.62; 95%可信区间[CI] 0.43-0.91; P=0.010)显著相关。使用粗数据的敏感性分析也支持死亡率获益(OR 0.68; 95% CI 0.54-0.85)。结论:休克小组管理可能改善CS患者的短期预后,然而,证据水平非常低。需要进一步的前瞻性研究来评估最佳的冲击小组组成和作用。
{"title":"Effectiveness of the Shock Team on Short-Term Outcomes in Patients With Cardiogenic Shock - Systematic Review and Meta-Analysis.","authors":"Marina Arai, Toru Kondo, Takahiro Nakashima, Hiroyuki Hanada, Katsutaka Hashiba, Takeshi Yamamoto, Naoki Nakayama, Jin Kirigaya, Tomoko Ishizu, Yumiko Hosoya, Aya Katasako-Yabumoto, Yusuke Okazaki, Masahiro Yamamoto, Kazuo Sakamoto, Takumi Osawa, Akihito Tanaka, Kunihiro Matsuo, Junichi Yamaguchi, Toshiaki Mano, Sunao Kojima, Teruo Noguchi, Yasushi Tsujimoto, Migaku Kikuchi, Toshikazu Funazaki, Yoshio Tahara, Hiroshi Nonogi, Tetsuya Matoba","doi":"10.1253/circrep.CR-25-0240","DOIUrl":"10.1253/circrep.CR-25-0240","url":null,"abstract":"<p><strong>Background: </strong>Recently, shock teams have been introduced to optimize cardiogenic shock (CS) care; however, their clinical benefits remain unclear. We conducted a systematic review and meta-analysis to assess whether management by a shock team improves outcomes in patients with CS.</p><p><strong>Methods and results: </strong>This meta-analysis was conducted according to the PRISMA guidelines. Studies comparing adults with CS managed with or without a shock team were identified from the PubMed, Web of Science, and Cochrane Library databases. The primary outcome was short-term mortality (cardiac intensive care unit, in-hospital, or 30-day mortality); the secondary outcome was bleeding. Of the 7 retrospective cohort studies that met the inclusion criteria, 3 without a critical risk of bias were included in the analysis. Shock team management was significantly associated with lower short-term mortality (odds ratio [OR] 0.52; 95% confidence interval [CI] 0.32-0.85; P=0.010) and bleeding complications (OR 0.62; 95% CI 0.43-0.91; P=0.010). Sensitivity analysis using crude data also supported the mortality benefit (OR 0.68; 95% CI 0.54-0.85; P<0.010). However, no randomized trials were included, and the certainty of evidence was rated very low owing to the risk of bias and inconsistency.</p><p><strong>Conclusions: </strong>Shock team management may improve short-term outcomes in patients with CS; however, the level of evidence is very low. Further prospective studies are needed to evaluate optimal shock team composition and roles.</p>","PeriodicalId":94305,"journal":{"name":"Circulation reports","volume":"8 1","pages":"13-20"},"PeriodicalIF":1.1,"publicationDate":"2025-11-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12782905/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145954804","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-11-12eCollection Date: 2026-01-09DOI: 10.1253/circrep.CR-25-0217
Tatsuhiro Shibata, Koshiro Kanaoka, Yoshitaka Iwanaga, Yoko Sumita, Satoaki Matoba, Masaki Ieda, Satoshi Yasuda, Shun Kohsaka, Tetsuya Matoba, Masaharu Nakayama, Tetsuya Amano, Yasuko K Bando, Mika Enomoto, Aya Saito, Hiroshi Tada, Yoshihiro Fukumoto
Background: Comprehensive monitoring of cardiovascular disease (CVD) is essential in rapidly aging societies such as Japan. The Japanese Circulation Society (JCS) launched the Japanese Registry Of All cardiac and vascular Diseases-Diagnosis Procedure Combination (JROAD-DPC) registry, linking annual JROAD questionnaires with nationwide DPC administrative claims to enable patient-level analyses of hospitalized CVD care. This Protocol Paper presents a comprehensive overview of the registry.
Methods and results: Using anonymized data (April 2012-March 2023), we described temporal trends in patient demographics, principal CVD diagnoses, major interventions, disease-specific severity, and hospital characteristics. From FY2012-FY2022, participating facilities increased from 610 to 860, with registered patients more than doubling. Median age rose from 73.0 to 75.0 years; patients aged ≥90 years nearly quadrupled. The proportion of angina pectoris admissions declined (26.8% to 11.7%), while absolute numbers remained stable. Atrial fibrillation/flutter admissions rose in both proportion (4.1% to 5.9%) and absolute number. Heart failure admissions increased steadily, with its proportion showing a U-shaped trend. Catheter ablations for atrial fibrillation/flutter increased over fivefold, exceeding 64,000, while percutaneous coronary interventions for acute myocardial infarction surpassed 46,000.
Conclusions: JROAD-DPC now captures over 1.5 million annual CVD hospitalizations, providing a nationwide, large-scale longitudinal view of cardiovascular care in Japan. Its scale and validated coding enable robust analyses of trends and outcomes, supporting national CVD policy evaluation and improvement.
{"title":"Design and Framework of JROAD-DPC - A Japanese Nationwide Registry Linking Diagnosis Procedure Combination Data With Cardiovascular Quality Metrics.","authors":"Tatsuhiro Shibata, Koshiro Kanaoka, Yoshitaka Iwanaga, Yoko Sumita, Satoaki Matoba, Masaki Ieda, Satoshi Yasuda, Shun Kohsaka, Tetsuya Matoba, Masaharu Nakayama, Tetsuya Amano, Yasuko K Bando, Mika Enomoto, Aya Saito, Hiroshi Tada, Yoshihiro Fukumoto","doi":"10.1253/circrep.CR-25-0217","DOIUrl":"10.1253/circrep.CR-25-0217","url":null,"abstract":"<p><strong>Background: </strong>Comprehensive monitoring of cardiovascular disease (CVD) is essential in rapidly aging societies such as Japan. The Japanese Circulation Society (JCS) launched the Japanese Registry Of All cardiac and vascular Diseases-Diagnosis Procedure Combination (JROAD-DPC) registry, linking annual JROAD questionnaires with nationwide DPC administrative claims to enable patient-level analyses of hospitalized CVD care. This Protocol Paper presents a comprehensive overview of the registry.</p><p><strong>Methods and results: </strong>Using anonymized data (April 2012-March 2023), we described temporal trends in patient demographics, principal CVD diagnoses, major interventions, disease-specific severity, and hospital characteristics. From FY2012-FY2022, participating facilities increased from 610 to 860, with registered patients more than doubling. Median age rose from 73.0 to 75.0 years; patients aged ≥90 years nearly quadrupled. The proportion of angina pectoris admissions declined (26.8% to 11.7%), while absolute numbers remained stable. Atrial fibrillation/flutter admissions rose in both proportion (4.1% to 5.9%) and absolute number. Heart failure admissions increased steadily, with its proportion showing a U-shaped trend. Catheter ablations for atrial fibrillation/flutter increased over fivefold, exceeding 64,000, while percutaneous coronary interventions for acute myocardial infarction surpassed 46,000.</p><p><strong>Conclusions: </strong>JROAD-DPC now captures over 1.5 million annual CVD hospitalizations, providing a nationwide, large-scale longitudinal view of cardiovascular care in Japan. Its scale and validated coding enable robust analyses of trends and outcomes, supporting national CVD policy evaluation and improvement.</p>","PeriodicalId":94305,"journal":{"name":"Circulation reports","volume":"8 1","pages":"180-189"},"PeriodicalIF":1.1,"publicationDate":"2025-11-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12782913/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145954779","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Background: B-type natriuretic peptide (BNP) is a key biomarker for heart failure (HF) and widely used for risk stratification. Elevated BNP levels in acute stroke are linked to poor outcomes, but its prognostic value in the post-acute phase remains unclear.
Methods and results: This retrospective study included 876 patients admitted to a rehabilitation hospital after acute cerebral infarction or hemorrhage between February 2019 and December 2022. Patients were classified into 4 groups based on BNP or N-terminal prohormone of BNP. The primary outcome was all-cause unfavorable events, including in-hospital death or transfer due to worsening condition. The severely elevated BNP group had a significantly higher risk of all-cause unfavorable events (hazard ratio: 2.34; 95% confidence interval: 1.26-4.32) than the normal group. No significant difference was observed in the mildly or moderately elevated BNP groups. BNP showed superior predictive value over HF diagnosis in terms of area under the receiver operating characteristic curve (0.712 vs. 0.691), net reclassification improvement (0.304, P=0.002), and integrated discrimination improvement (0.025, P=0.015). Higher BNP was associated with lower body mass index, reduced estimated glomerular filtration rate, longer time from stroke onset, atrial fibrillation, and cardioembolic stroke.
Conclusions: BNP levels in the post-acute stroke phase were significantly associated with unfavorable outcomes and may serve as a useful prognostic marker.
背景:b型利钠肽(BNP)是心衰(HF)的关键生物标志物,被广泛用于危险分层。急性卒中中BNP水平升高与预后不良有关,但其在急性期后的预后价值尚不清楚。方法和结果:本回顾性研究纳入2019年2月至2022年12月期间入院的876例急性脑梗死或出血患者。根据BNP或n端原激素水平将患者分为4组。主要结局为全因不良事件,包括院内死亡或因病情恶化而转院。BNP严重升高组发生全因不良事件的风险显著高于正常组(风险比:2.34;95%可信区间:1.26-4.32)。轻度或中度BNP升高组无显著差异。BNP在受试者工作特征曲线下面积(0.712 vs. 0.691)、净重分类改善(0.304,P=0.002)和综合判别改善(0.025,P=0.015)方面优于HF诊断的预测价值。高BNP与较低的身体质量指数、较低的肾小球滤过率、较长的中风发病时间、心房颤动和心脏栓塞性中风相关。结论:急性卒中后阶段BNP水平与不良预后显著相关,可作为有用的预后指标。
{"title":"Elevated B-Type Natriuretic Peptide as a Predictor of Unfavorable Outcomes in Post-Acute Stroke Patients.","authors":"Genki Kai, Ken Ogura, Kensuke Ueno, Kaoru Sato, Takashi Miki, Takumi Noda, Masashi Yamashita, Masashi Kanai, Masafumi Nozoe, Kentaro Kamiya","doi":"10.1253/circrep.CR-25-0132","DOIUrl":"10.1253/circrep.CR-25-0132","url":null,"abstract":"<p><strong>Background: </strong>B-type natriuretic peptide (BNP) is a key biomarker for heart failure (HF) and widely used for risk stratification. Elevated BNP levels in acute stroke are linked to poor outcomes, but its prognostic value in the post-acute phase remains unclear.</p><p><strong>Methods and results: </strong>This retrospective study included 876 patients admitted to a rehabilitation hospital after acute cerebral infarction or hemorrhage between February 2019 and December 2022. Patients were classified into 4 groups based on BNP or N-terminal prohormone of BNP. The primary outcome was all-cause unfavorable events, including in-hospital death or transfer due to worsening condition. The severely elevated BNP group had a significantly higher risk of all-cause unfavorable events (hazard ratio: 2.34; 95% confidence interval: 1.26-4.32) than the normal group. No significant difference was observed in the mildly or moderately elevated BNP groups. BNP showed superior predictive value over HF diagnosis in terms of area under the receiver operating characteristic curve (0.712 vs. 0.691), net reclassification improvement (0.304, P=0.002), and integrated discrimination improvement (0.025, P=0.015). Higher BNP was associated with lower body mass index, reduced estimated glomerular filtration rate, longer time from stroke onset, atrial fibrillation, and cardioembolic stroke.</p><p><strong>Conclusions: </strong>BNP levels in the post-acute stroke phase were significantly associated with unfavorable outcomes and may serve as a useful prognostic marker.</p>","PeriodicalId":94305,"journal":{"name":"Circulation reports","volume":"8 1","pages":"144-152"},"PeriodicalIF":1.1,"publicationDate":"2025-11-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12782912/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145954822","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Background: Studies of off-loading devices for chronic limb-threatening ischemia (CLTI) are scarce. We investigated (1) the effect of the application of early therapy sandals on changes in the Clinical Frailty Scale (CFS) scores of patients with CLTI before and after hospitalization, and (2) adverse events such as wound deterioration and reamputation.
Methods and results: We retrospectively analyzed the cases of 51 patients (51 limbs) with toe amputation after revascularization and compared 2 groups: patients who did not apply any load during the off-loading duration and focused on resistance training (the 'usual rehabilitation' group), and those who used therapeutic sandals and performed walking and aerobic exercises with partial off-loading from an early stage (the 'orthotic' rehabilitation group). The before-to-after hospitalization change in the CFS score was 0 (-1, 0) in the usual rehabilitation group, and 0 (0, 1) in the orthotic rehabilitation group (P=0.002), a significant difference. There were no significant between-group differences in wound healing duration (usual rehabilitation group, 48 [19,76.5] days; orthotic rehabilitation group, 41 [27.5,78.8] days) or reamputation rate (usual rehabilitation group, 5 [22%]; orthotic rehabilitation group, 3 [11%]).
Conclusions: The early postoperative use of therapeutic sandals tended to shorten the duration of complete off-loading after toe amputation due to CLTI and to help maintain CFS scores throughout the hospitalization duration. It was also shown to have a minimal impact on treatment delay and reamputation.
{"title":"Effects of Rehabilitation Using Therapeutic Sandals for Patients With Chronic Limb-Threatening Ischemia.","authors":"Yusuke Nakamura, Takuya Hara, Manami Kurozawa, Kou Ino, Takashi Matsumoto","doi":"10.1253/circrep.CR-25-0048","DOIUrl":"10.1253/circrep.CR-25-0048","url":null,"abstract":"<p><strong>Background: </strong>Studies of off-loading devices for chronic limb-threatening ischemia (CLTI) are scarce. We investigated (1) the effect of the application of early therapy sandals on changes in the Clinical Frailty Scale (CFS) scores of patients with CLTI before and after hospitalization, and (2) adverse events such as wound deterioration and reamputation.</p><p><strong>Methods and results: </strong>We retrospectively analyzed the cases of 51 patients (51 limbs) with toe amputation after revascularization and compared 2 groups: patients who did not apply any load during the off-loading duration and focused on resistance training (the 'usual rehabilitation' group), and those who used therapeutic sandals and performed walking and aerobic exercises with partial off-loading from an early stage (the 'orthotic' rehabilitation group). The before-to-after hospitalization change in the CFS score was 0 (-1, 0) in the usual rehabilitation group, and 0 (0, 1) in the orthotic rehabilitation group (P=0.002), a significant difference. There were no significant between-group differences in wound healing duration (usual rehabilitation group, 48 [19,76.5] days; orthotic rehabilitation group, 41 [27.5,78.8] days) or reamputation rate (usual rehabilitation group, 5 [22%]; orthotic rehabilitation group, 3 [11%]).</p><p><strong>Conclusions: </strong>The early postoperative use of therapeutic sandals tended to shorten the duration of complete off-loading after toe amputation due to CLTI and to help maintain CFS scores throughout the hospitalization duration. It was also shown to have a minimal impact on treatment delay and reamputation.</p>","PeriodicalId":94305,"journal":{"name":"Circulation reports","volume":"8 1","pages":"136-143"},"PeriodicalIF":1.1,"publicationDate":"2025-11-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12782914/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145954845","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Background: Catheter ablation (CA) is a well-established therapy for arrhythmia, but the impact of CA strategies has not been thoroughly investigated. Nagano Prefecture comprises a large geographical area and some hospitals do not have cardiac surgeons, thus limiting the application of CA strategies. The aim of this study was to investigate the detailed strategies for CA in Nagano Prefecture and to clarify their efficacy and safety.
Methods and results: The Shinshu Catheter Ablation (Shinshu-AB) Registry is a multicenter prospective observational registry. Patients treated with CA for any type of arrhythmia are included. Data on the target arrhythmia(s), CA strategy, outcomes, and complications were collected and analyzed at Shinshu University Hospital. The study was approved by the institutional review boards of all investigational sites and registered in the UMIN Clinical Trials Registry (UMIN-55562). Primary endpoints were the composite incidence of arrhythmia recurrence, procedure-related adverse events, and cardiovascular events. The secondary endpoints were acute success, chronic success for >12 months, and all-cause death.
Conclusions: The Shinshu-AB Registry provides real-world data from the Nagano Prefecture on the outcomes and complications of CA for various types of arrhythmias.
{"title":"Registry for Long-Term Outcomes After Catheter Ablation in Nagano Prefecture - The Shinshu Catheter Ablation (Shinshu-AB) Registry Rationale and Design.","authors":"Toshinori Komatsu, Ayako Okada, Hideki Kobayashi, Kiu Tanaka, Hiroaki Tabata, Wataru Shoin, Toshio Kasai, Takahiro Okano, Tatsuya Usui, Yasumasa Nohno, Ryosuke Kozu, Hideaki Sato, Takeshi Tomita, Takahiro Takeuchi, Masao Hirabayashi, Kazunori Aizawa, Yasutaka Oguchi, Yuichi Katagiri, Yasushi Wakabayashi, Koichiro Kuwahara","doi":"10.1253/circrep.CR-25-0229","DOIUrl":"10.1253/circrep.CR-25-0229","url":null,"abstract":"<p><strong>Background: </strong>Catheter ablation (CA) is a well-established therapy for arrhythmia, but the impact of CA strategies has not been thoroughly investigated. Nagano Prefecture comprises a large geographical area and some hospitals do not have cardiac surgeons, thus limiting the application of CA strategies. The aim of this study was to investigate the detailed strategies for CA in Nagano Prefecture and to clarify their efficacy and safety.</p><p><strong>Methods and results: </strong>The Shinshu Catheter Ablation (Shinshu-AB) Registry is a multicenter prospective observational registry. Patients treated with CA for any type of arrhythmia are included. Data on the target arrhythmia(s), CA strategy, outcomes, and complications were collected and analyzed at Shinshu University Hospital. The study was approved by the institutional review boards of all investigational sites and registered in the UMIN Clinical Trials Registry (UMIN-55562). Primary endpoints were the composite incidence of arrhythmia recurrence, procedure-related adverse events, and cardiovascular events. The secondary endpoints were acute success, chronic success for >12 months, and all-cause death.</p><p><strong>Conclusions: </strong>The Shinshu-AB Registry provides real-world data from the Nagano Prefecture on the outcomes and complications of CA for various types of arrhythmias.</p>","PeriodicalId":94305,"journal":{"name":"Circulation reports","volume":"8 1","pages":"174-179"},"PeriodicalIF":1.1,"publicationDate":"2025-11-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12783018/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145954834","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Background: Although metabolic dysfunction-associated fatty liver disease is typically diagnosed using ultrasonography, the fatty liver index (FLI) offers a simple alternative. Brachial-ankle pulse wave velocity (baPWV) is an established marker of arterial stiffness and a predictor of cardiovascular events. This study investigated the association between FLI and baPWV in a general Japanese population.
Methods and results: This cross-sectional study included participants aged ≥18 years, excluding those with atrial fibrillation, lower extremity artery disease, severe aortic stenosis, or missing data. The primary outcome was an elevated baPWV (≥1,800 cm/s). Multivariable logistic regression analysis was performed to assess the association between FLI and elevated baPWV, considering FLI both as a categorical variable (low risk: FLI <30; moderate risk: FLI ≥30 and <60; high risk: FLI ≥60) and as a continuous variable (per 10-unit increase). The analysis included 10,122 individuals (mean age 54.3 years; 55% male). In multivariable-adjusted models, the odds of elevated baPWV were significantly higher in the moderate-risk (odds ratio [OR] 1.47; 95% confidence interval [CI] 1.20-1.79) and high-risk (OR 1.78; 95% CI 1.33-2.38) groups, using the low-risk group as the reference category. Each 10-unit increase in FLI was associated with significantly higher odds of the outcome (OR 1.16; 95% CI 1.10-1.22).
Conclusions: FLI showed a significant association with arterial stiffness in the general Japanese population.
{"title":"Association Between Fatty Liver Index and Brachial-Ankle Pulse Wave Velocity in the General Population - A Cross-Sectional Study.","authors":"Daisuke Tokutake, Yuichi Akasaki, Shuya Shinchi, Shota Uebo, Shin Kawasoe, Takuro Kubozono, Hironori Miyahara, Koichi Tokushige, Mitsuru Ohishi","doi":"10.1253/circrep.CR-25-0218","DOIUrl":"10.1253/circrep.CR-25-0218","url":null,"abstract":"<p><strong>Background: </strong>Although metabolic dysfunction-associated fatty liver disease is typically diagnosed using ultrasonography, the fatty liver index (FLI) offers a simple alternative. Brachial-ankle pulse wave velocity (baPWV) is an established marker of arterial stiffness and a predictor of cardiovascular events. This study investigated the association between FLI and baPWV in a general Japanese population.</p><p><strong>Methods and results: </strong>This cross-sectional study included participants aged ≥18 years, excluding those with atrial fibrillation, lower extremity artery disease, severe aortic stenosis, or missing data. The primary outcome was an elevated baPWV (≥1,800 cm/s). Multivariable logistic regression analysis was performed to assess the association between FLI and elevated baPWV, considering FLI both as a categorical variable (low risk: FLI <30; moderate risk: FLI ≥30 and <60; high risk: FLI ≥60) and as a continuous variable (per 10-unit increase). The analysis included 10,122 individuals (mean age 54.3 years; 55% male). In multivariable-adjusted models, the odds of elevated baPWV were significantly higher in the moderate-risk (odds ratio [OR] 1.47; 95% confidence interval [CI] 1.20-1.79) and high-risk (OR 1.78; 95% CI 1.33-2.38) groups, using the low-risk group as the reference category. Each 10-unit increase in FLI was associated with significantly higher odds of the outcome (OR 1.16; 95% CI 1.10-1.22).</p><p><strong>Conclusions: </strong>FLI showed a significant association with arterial stiffness in the general Japanese population.</p>","PeriodicalId":94305,"journal":{"name":"Circulation reports","volume":"8 1","pages":"118-126"},"PeriodicalIF":1.1,"publicationDate":"2025-11-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12795637/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145967130","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Background: The advent of transcatheter aortic valve implantation (TAVI) has increased the rate of aortic valve treatment in frail older adults. Factors contributing to frailty include sarcopenia (characterized by reduced muscle mass), osteopenia (characterized by decreased bone mineral density), and the newly termed osteosarcopenia, which is characterized by a simultaneous decline in muscle mass and bone mineral density. In this study, we aimed to investigate the impacts of sarcopenia, osteopenia, and osteosarcopenia on the clinical outcomes of TAVI.
Methods and results: We retrospectively analyzed 490 patients who underwent TAVI for aortic stenosis at Yamaguchi University Hospital between April 2014 and March 2025. Osteopenia, sarcopenia, and osteosarcopenia were diagnosed by preprocedural computed tomography. Patients were classified into normal (N), sarcopenia alone (S), osteopenia alone (O), and osteosarcopenia (OS) groups. Early clinical outcomes and 1-year survival rates exhibited no significant differences among the groups. However, the 5-year survival rates were 94.1%, 77.6%, 60.4%, and 46.5% in the N, S, O, and OS groups, respectively (P<0.05). The Cox proportional hazards model revealed osteosarcopenia as a significant risk factor for late death (hazard ratio, 2.09; P=0.0002).
Conclusions: Preoperative evaluation of muscle mass and bone density aids in stratifying TAVI risk.
{"title":"Impacts of Sarcopenia, Osteopenia, and Osteosarcopenia on Patients Undergoing Transcatheter Aortic Valve Implantation - A Single-Center Retrospective Cohort Study.","authors":"Hiroshi Kurazumi, Ryo Suzuki, Takato Nakashima, Ryosuke Nawata, Toshiki Yokoyama, Kazumasa Matsunaga, Yosuke Miyazaki, Atsuo Yamashita, Takayuki Okamura, Akihito Mikamo, Motoaki Sano, Kimikazu Hamano","doi":"10.1253/circrep.CR-25-0190","DOIUrl":"10.1253/circrep.CR-25-0190","url":null,"abstract":"<p><strong>Background: </strong>The advent of transcatheter aortic valve implantation (TAVI) has increased the rate of aortic valve treatment in frail older adults. Factors contributing to frailty include sarcopenia (characterized by reduced muscle mass), osteopenia (characterized by decreased bone mineral density), and the newly termed osteosarcopenia, which is characterized by a simultaneous decline in muscle mass and bone mineral density. In this study, we aimed to investigate the impacts of sarcopenia, osteopenia, and osteosarcopenia on the clinical outcomes of TAVI.</p><p><strong>Methods and results: </strong>We retrospectively analyzed 490 patients who underwent TAVI for aortic stenosis at Yamaguchi University Hospital between April 2014 and March 2025. Osteopenia, sarcopenia, and osteosarcopenia were diagnosed by preprocedural computed tomography. Patients were classified into normal (N), sarcopenia alone (S), osteopenia alone (O), and osteosarcopenia (OS) groups. Early clinical outcomes and 1-year survival rates exhibited no significant differences among the groups. However, the 5-year survival rates were 94.1%, 77.6%, 60.4%, and 46.5% in the N, S, O, and OS groups, respectively (P<0.05). The Cox proportional hazards model revealed osteosarcopenia as a significant risk factor for late death (hazard ratio, 2.09; P=0.0002).</p><p><strong>Conclusions: </strong>Preoperative evaluation of muscle mass and bone density aids in stratifying TAVI risk.</p>","PeriodicalId":94305,"journal":{"name":"Circulation reports","volume":"8 1","pages":"93-102"},"PeriodicalIF":1.1,"publicationDate":"2025-11-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12795636/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145967346","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Background: Because the optimal choice of vasopressor for the initial treatment of cardiogenic shock (CS) remains controversial, we conducted a systematic review and meta-analysis to evaluate whether noradrenaline improves clinical outcomes compared with other vasopressors (adrenaline, dopamine, and vasopressin) in patients with CS.
Methods and results: PubMed, CENTRAL, and Web of Science databases were searched for randomized controlled trials (RCTs) and observational studies comparing noradrenaline with other vasopressors in adults with CS. A meta-analysis was conducted using fixed-effect models where appropriate. Two RCTs were included (n=337). One trial enrolled 57 patients and compared the effects of noradrenaline and adrenaline. Another study included 280 patients with CS as a subgroup and compared noradrenaline with dopamine. Pooled analysis showed that noradrenaline likely reduced the 28-day mortality rate compared with other vasopressors (very-low certainty). This corresponded to approximately 110 fewer deaths per 1000 patients (95% confidence interval: 217 fewer to 5 fewer). Secondary outcomes from the Levy study indicated fewer adverse events in the noradrenaline group.
Conclusions: Noradrenaline likely reduces the 28-day mortality rate compared with other vasopressors (very-low certainty) in CS. Given the small number of studies and the potential bias, further large-scale trials are warranted.
背景:由于心脏源性休克(CS)初始治疗血管加压素的最佳选择仍然存在争议,我们进行了一项系统回顾和荟萃分析,以评估与其他血管加压素(肾上腺素、多巴胺和血管加压素)相比,去甲肾上腺素是否能改善CS患者的临床结果。方法和结果:检索PubMed、CENTRAL和Web of Science数据库,查找随机对照试验(rct)和观察性研究,比较去甲肾上腺素与其他血管加压药物在成人CS中的作用。适当时使用固定效应模型进行meta分析。纳入两项随机对照试验(n=337)。一项试验招募了57名患者,比较去甲肾上腺素和肾上腺素的效果。另一项研究将280名CS患者作为亚组,并将去甲肾上腺素与多巴胺进行比较。综合分析显示,与其他血管加压药物相比,去甲肾上腺素可能降低28天死亡率(非常低的确定性)。这相当于每1000名患者死亡人数减少约110人(95%置信区间:减少217人至减少5人)。利维研究的次要结果表明,去甲肾上腺素组的不良事件较少。结论:与其他血管加压药物相比,去甲肾上腺素可能降低CS患者的28天死亡率(非常低的确定性)。考虑到研究数量少和潜在的偏倚,进一步的大规模试验是有必要的。
{"title":"Comparative Efficacy of Noradrenaline vs. Other Vasopressors on Outcomes in Patients With Cardiogenic Shock - A Systematic Review and Meta-Analysis.","authors":"Yumiko Hosoya, Masahiro Yamamoto, Hiroyuki Hanada, Takumi Osawa, Marina Arai, Kazuo Sakamoto, Yusuke Okazaki, Aya Katasako-Yabumoto, Tomoko Ishizu, Toru Kondo, Jin Kirigaya, Naoki Nakayama, Takeshi Yamamoto, Katsutaka Hashiba, Takahiro Nakashima, Teruo Noguchi, Yasushi Tsujimoto, Migaku Kikuchi, Toshikazu Funazaki, Yoshio Tahara, Hiroshi Nonogi, Tetsuya Matoba","doi":"10.1253/circrep.CR-25-0188","DOIUrl":"10.1253/circrep.CR-25-0188","url":null,"abstract":"<p><strong>Background: </strong>Because the optimal choice of vasopressor for the initial treatment of cardiogenic shock (CS) remains controversial, we conducted a systematic review and meta-analysis to evaluate whether noradrenaline improves clinical outcomes compared with other vasopressors (adrenaline, dopamine, and vasopressin) in patients with CS.</p><p><strong>Methods and results: </strong>PubMed, CENTRAL, and Web of Science databases were searched for randomized controlled trials (RCTs) and observational studies comparing noradrenaline with other vasopressors in adults with CS. A meta-analysis was conducted using fixed-effect models where appropriate. Two RCTs were included (n=337). One trial enrolled 57 patients and compared the effects of noradrenaline and adrenaline. Another study included 280 patients with CS as a subgroup and compared noradrenaline with dopamine. Pooled analysis showed that noradrenaline likely reduced the 28-day mortality rate compared with other vasopressors (very-low certainty). This corresponded to approximately 110 fewer deaths per 1000 patients (95% confidence interval: 217 fewer to 5 fewer). Secondary outcomes from the Levy study indicated fewer adverse events in the noradrenaline group.</p><p><strong>Conclusions: </strong>Noradrenaline likely reduces the 28-day mortality rate compared with other vasopressors (very-low certainty) in CS. Given the small number of studies and the potential bias, further large-scale trials are warranted.</p>","PeriodicalId":94305,"journal":{"name":"Circulation reports","volume":"7 12","pages":"1154-1161"},"PeriodicalIF":1.1,"publicationDate":"2025-11-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12688426/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145728023","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Background: Enteral nutrition (EN) is often delayed in critically ill cardiovascular patients due to concerns about bowel ischemia, especially when under vasopressor or mechanical support. We evaluated the impact of a structured EN protocol designed to promote timely and safe nutrition delivery in the Cardiac Care Unit (CCU).
Methods and results: This single-center retrospective study compared mechanically ventilated CCU patients before (April 2019-March 2020) and after (April 2022-March 2023) protocol implementation. The protocol specified hemodynamic safety thresholds and used a peptide-based formula. Outcomes included EN-related complications, time to EN initiation, and nutritional adequacy within the first week. A total of 116 patients (58 per group) were analyzed. No significant differences were observed in vomiting (P=0.717), diarrhea (P=0.219), or bowel ischemia (P=0.364). The post-protocol group showed a significantly shorter time to EN initiation (median 39.5 vs. 76.0 h; P<0.001). By Day 5, enteral energy adequacy improved (40.8% vs. 12.3%; P<0.001), and protein adequacy increased (62.2% vs. 31.0%; P<0.001). Exploratory analyses showed no significant differences in CCU stay, ventilator-free days, or in-hospital deaths.
Conclusions: The EN protocol enabled earlier initiation and improved EN delivery in high-risk CCU patients without increasing complications, offering a safe and practical approach to narrowing the gap between guidelines and practice.
背景:由于担心肠缺血,肠内营养(EN)在危重心血管患者中经常被延迟,特别是在血管加压或机械支持下。我们评估了一个结构化的EN方案的影响,该方案旨在促进心脏护理病房(CCU)及时和安全的营养输送。方法和结果:本单中心回顾性研究比较了机械通气CCU患者在方案实施前(2019年4月- 2020年3月)和实施后(2022年4月- 2023年3月)的情况。该方案规定了血流动力学安全阈值,并使用了基于肽的配方。结果包括EN相关并发症、EN起始时间和第一周内的营养充足性。共分析116例患者(每组58例)。呕吐(P=0.717)、腹泻(P=0.219)、肠缺血(P=0.364)无显著性差异。方案后组的EN起始时间明显缩短(中位数为39.5 h vs. 76.0 h)。结论:EN方案能够在不增加并发症的情况下使高危CCU患者更早起始并改善EN交付,为缩小指南与实践之间的差距提供了一种安全实用的方法。
{"title":"Implementation of an Enteral Nutrition Protocol in the Cardiac Care Unit - A Retrospective Study of Critically Ill Cardiovascular Patients.","authors":"Tadakiyo Ido, Takaharu Hayashi, Tomoki Yamada, Kei Nakamoto, Yohei Sotomi, Yoshiharu Higuchi","doi":"10.1253/circrep.CR-25-0113","DOIUrl":"10.1253/circrep.CR-25-0113","url":null,"abstract":"<p><strong>Background: </strong>Enteral nutrition (EN) is often delayed in critically ill cardiovascular patients due to concerns about bowel ischemia, especially when under vasopressor or mechanical support. We evaluated the impact of a structured EN protocol designed to promote timely and safe nutrition delivery in the Cardiac Care Unit (CCU).</p><p><strong>Methods and results: </strong>This single-center retrospective study compared mechanically ventilated CCU patients before (April 2019-March 2020) and after (April 2022-March 2023) protocol implementation. The protocol specified hemodynamic safety thresholds and used a peptide-based formula. Outcomes included EN-related complications, time to EN initiation, and nutritional adequacy within the first week. A total of 116 patients (58 per group) were analyzed. No significant differences were observed in vomiting (P=0.717), diarrhea (P=0.219), or bowel ischemia (P=0.364). The post-protocol group showed a significantly shorter time to EN initiation (median 39.5 vs. 76.0 h; P<0.001). By Day 5, enteral energy adequacy improved (40.8% vs. 12.3%; P<0.001), and protein adequacy increased (62.2% vs. 31.0%; P<0.001). Exploratory analyses showed no significant differences in CCU stay, ventilator-free days, or in-hospital deaths.</p><p><strong>Conclusions: </strong>The EN protocol enabled earlier initiation and improved EN delivery in high-risk CCU patients without increasing complications, offering a safe and practical approach to narrowing the gap between guidelines and practice.</p>","PeriodicalId":94305,"journal":{"name":"Circulation reports","volume":"8 1","pages":"127-135"},"PeriodicalIF":1.1,"publicationDate":"2025-11-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12782910/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145954837","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Background: Managing heart failure complicated by severe right heart failure with implantable mechanical circulatory support remains a significant challenge. One therapeutic strategy is biventricular assist device (BiVAD) support, typically involving the off-label use of 2 implantable left ventricular assist devices (LVADs). Because the available data of implantable BiVAD support remain limited, we reviewed the data for 6 patients on implantable BiVAD support.
Methods and results: Between January 2010 and March 2019, 6 patients underwent BiVAD implantation at Osaka University Hospital. Their mean age was 31±11 years, and 2 (33%) were male. The right ventricular assist devices (RVADs) utilized were Jarvik2000 (Jarvik Heart, NY, USA) in 4 patients (67%), and HVAD (HeartWare, Framingham, MA, USA) in 2 patients (33%). The survival rates at 1 and 3 years after BiVAD implantation were 83% and 67%, respectively. Of the 6 patients, 4 underwent heart transplantation at 553, 709, 791, and 1,245 days, respectively, following RVAD implantation; 2 patients died during follow-up at 280 and 511 days, respectively, after RVAD implantation. Stroke occurred in 3 patients. Hemolysis or pump thrombosis occurred in 3 patients. Heart failure occurred in 3 patients. Device-related infection occurred in 1 patient.
Conclusions: Although implantable BiVAD support provided a feasible bridge to transplantation with favorable survival, the high incidence of complications indicates that significant challenges remain in optimizing patient outcomes and emphasizes the necessity for RV-specific device development.
{"title":"Long-Term Implantable Biventricular Assist Device Support - Experience of 6 Cases.","authors":"Shusuke Imaoka, Shunsuke Saito, Daisuke Yoshioka, Takuji Kawamura, Ai Kawamura, Shin Yajima, Ryohei Matsuura, Yusuke Misumi, Shigeru Miyagawa","doi":"10.1253/circrep.CR-25-0224","DOIUrl":"10.1253/circrep.CR-25-0224","url":null,"abstract":"<p><strong>Background: </strong>Managing heart failure complicated by severe right heart failure with implantable mechanical circulatory support remains a significant challenge. One therapeutic strategy is biventricular assist device (BiVAD) support, typically involving the off-label use of 2 implantable left ventricular assist devices (LVADs). Because the available data of implantable BiVAD support remain limited, we reviewed the data for 6 patients on implantable BiVAD support.</p><p><strong>Methods and results: </strong>Between January 2010 and March 2019, 6 patients underwent BiVAD implantation at Osaka University Hospital. Their mean age was 31±11 years, and 2 (33%) were male. The right ventricular assist devices (RVADs) utilized were Jarvik2000 (Jarvik Heart, NY, USA) in 4 patients (67%), and HVAD (HeartWare, Framingham, MA, USA) in 2 patients (33%). The survival rates at 1 and 3 years after BiVAD implantation were 83% and 67%, respectively. Of the 6 patients, 4 underwent heart transplantation at 553, 709, 791, and 1,245 days, respectively, following RVAD implantation; 2 patients died during follow-up at 280 and 511 days, respectively, after RVAD implantation. Stroke occurred in 3 patients. Hemolysis or pump thrombosis occurred in 3 patients. Heart failure occurred in 3 patients. Device-related infection occurred in 1 patient.</p><p><strong>Conclusions: </strong>Although implantable BiVAD support provided a feasible bridge to transplantation with favorable survival, the high incidence of complications indicates that significant challenges remain in optimizing patient outcomes and emphasizes the necessity for RV-specific device development.</p>","PeriodicalId":94305,"journal":{"name":"Circulation reports","volume":"8 1","pages":"103-109"},"PeriodicalIF":1.1,"publicationDate":"2025-11-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12782911/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145954765","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}